Releasing pharmaceutical products to the market is one of the most critical steps in terms of patient safety. High quality standards and strict adherence to regulatory-enforced batch certification processes are non-negotiable.

The heavily scrutinised batch disposition process leads to an overload of manual checks and ultimately a slowed-down product supply. Built on the Veeva QMS platform, Veeva Batch Release brings all relevant data into one place – making release-by-exception possible and reducing hours of QA effort to seconds.

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What typically gets in the way of accelerated batch releases:

• Release decisions dependent on fragmented data scattered across 10+ disconnected systems
• Manual checklists that consume hours of QA time per batch
• No system-supported visibility into market-specific requirements when performing batch reviews and dispositions
• Custom batch cockpit solutions that rely on complex and fragile integrations, leading to poor performance
• Time-consuming retrieval of batch-relevant data when retrospectively needed for investigations of quality events like product technical complaints